Results 61 to 70 of about 44,755 (204)

Data on the purification and crystallization of the loss-of-function von Willebrand disease variant (p.Gly1324Ser) of the von Willebrand factor A1 domain

Data in Brief, 2016
von Willebrand factor׳s (VWF) primary hemostatic responsibility is to deposit platelets at sites of vascular injury to prevent bleeding. This function is mediated by the interaction between the VWF A1 domain and the constitutively active platelet ...
James C. Campbell, Alexander Tischer, Venkata Machha, Laurie Moon-Tasson, Banumathi Sankaran, Choel Kim, Matthew Auton   +6 more
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Textbook of von Willebrand Disease : Basic and Clinical Aspects

Comprehensive resource summarizing recent research on von Willebrand disease, showing clinicians how to optimize management of patients with this disorder The newly revised and updated second edition of Textbook of von Willebrand Disease: Basic and ...
Federici, Augusto B., Montgomery, Robert R., Montgomery, Robert R.,, Berntorp, Erik E.,, Lillicrap, David,, Lillicrap, David, Federici, Augusto B.,, Lund University., Berntorp, Erik E.   +8 more
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Endovenous laser ablation of the great saphenous vein in patients with von willebrand disease

, 2013
Introduction Patients with von Willebrand disease have a high risk of bleeding during the surgical treatment of varicose veins. Endovenous laser ablation (EVLA) of the great saphenous vein (GSV) is a minimally invasive treatment for saphenofemoral ...
Sretenovic Z., Sretenovic J., Djurdjevic, Predrag, Novakovic, Sladjana B., Mirkovic N.   +4 more
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Choroba von Willebranda – najczęstsza osoczowa skaza krwotoczna

Menopause Review, 2010
Von Willebrand disease is the most common hereditary haemorrhagic disorder. A majority of patients (70%)have classic mild or moderate (type I) von Willebrand disease, and women are mostly affected.
Bożena Sokołowska
doaj  

von Willebrand Disease Associated with Superficial Temporal Artery Pseudoaneurysm

, 2005
We report on two patients with von Willebrand disease (vWD) that presented with superficial temporal artery pseudoaneurysms following minor blunt trauma. We discuss the possible pathophysiological link between vWD and blood vessel abnormalities.
Mwipatayi, B.P., Sieunarine, K., Eikelboom, J.W., Ricciardo, B.J., Abbas, M.   +4 more
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Identification and characterization of novel variations in platelet G-protein coupled receptor (GPCR) genes in patients historically diagnosed with type 1 von Willebrand disease : GPCR variations in type 1 von Willebrand disease [PDF]

, 2015
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other mild bleeding diatheses. We previously showed that mutations in the platelet P2Y12 ADP receptor gene (P2RY12) could contribute to the bleeding phenotype ...
F. Hill, Watson, Steve P., Goodeve Anne C., Goodeve, Anne C., Stockley Jacqueline, Lethagen Stefan, V. C. Leo, S. Lethagen, Sabi Essa, Daly Martina E., Daly, M.E., Mundell, S.J., S. P. Nisar, Leo Vincenzo C., Cunningham, Margaret R, E. Sabi, Schneppenheim, R., D. Habart, A. Tosetto, J. Goudemand, Daly, Martina E., Cunningham Margaret R., I. Peake, C. Mazurier, Lethagen, S., Eikenboom, Jeroen C, GAPP Study in Collaboration with the MCMDM-1VWD Study Group, E. Fressinaud, Leo, V.C., Margaret R Cunningham, Stuart J Mundell, Eikenboom, J.C., Reinhard Schneppenheim, Vincenzo C Leo, Nisar, Shaista P, Leo, Vincenzo C., Shaista P Nisar, S. J. Mundell, U. Budde, Nisar Shaista P., on behalf of the GAPP study in collaboration with the MCMDM-1VWD study group, Martina E Daly, Goodeve, Anne C, Leo, Vincenzo C, Nisar, Shaista P., , on behalf of the GAPP study in collaboration with the MCMDM-1VWD, Daly, Martina E, Cunningham, M.R., Essa Sabi, D. Meyer, Watson, S.P., Jeroen C Eikenboom, Schneppenheim, Reinhard, F. Rodeghiero, Steve P Watson, Nisar, S.P., Mundell, Stuart J, Cunningham, Margaret R., Mundell, Stuart J., Jacqueline Stockley, G. Castaman, J. Pasi, Eikenboom Jeroen C., J. Stockley, L. Holmberg, Stockley, J., Stockley, Jacqueline, Sabi, Essa, J. Ingerslev, Lethagen, Stefan, Watson Steve P., Stefan Lethagen, Z. Vorlova, Anne C Goodeve, Sabi, E., S. P. Watson, J. C. Eikenboom, Eikenboom, Jeroen C., Goodeve, A.C., R. Schneppenheim, M. R. Cunningham, Mundell Stuart J., Schneppenheim Reinhard, A.B. Federici, A. C. Goodeve, M. E. Daly, Watson, Steve P; id_orcid, J. Batlle   +87 more
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Impaired megakaryocytopoiesis in type 2B von Willebrand disease

, 2006
In this issue, Nurden and colleagues provide evidence that the severe thrombocytopenia found in a family with type 2B von Willebrand disease (VWD) is due also to impaired megakaryocytopoiesis, as shown both by changes in proteins involved in platelet ...
A.B. Federici
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Polymorphism in the promoter region of von Willebrand factor gene and von Willebrand disease type 1

Genetics and Molecular Biology, 2003
The -1185A/G polymorphism in the 5'-regulatory region of the von Willebrand factor (VWF) gene was associated with VWF plasma levels in a normal population.
Daniel Simon, Eliane Bandinelli, Israel Roisenberg   +2 more
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Weibel-Palade body formation and exocytosis in von Willebrand disease

, 2013
The studies presented in this thesis explored several pathogenic mechanisms underlying von Willebrand disease that is characterized by a quantitative or functional deficiency of von Willebrand factor, in particular with respect to intracellular storage ...
Wang, J.W.
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Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease [PDF]

, 2016
The heterogeneity of von Willebrand disease (VWD) makes its diagnosis a difficult ...
ROMUALDI, CHIARA, G. Barbon, V. Daidone, I. Di Pasquale, BARBON, GIOVANNI, C. Romualdi, E. Pontara, DAIDONE, VIVIANA, PONTARA, ELENA, Hosokawa, K, A. Casonato, PELOSO CATTINI, MARIA GRAZIA, K. Hosokawa, CASONATO, SANDRA, M. G. Cattini, DI PASQUALE, IRENE   +15 more
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